US4908161A - Fire retardant for isocyanate-based foams comprising ammonium sulfate and a cyanuric acid derivative - Google Patents

Fire retardant for isocyanate-based foams comprising ammonium sulfate and a cyanuric acid derivative Download PDF

Info

Publication number
US4908161A
US4908161A US07/210,748 US21074888A US4908161A US 4908161 A US4908161 A US 4908161A US 21074888 A US21074888 A US 21074888A US 4908161 A US4908161 A US 4908161A
Authority
US
United States
Prior art keywords
foams
isocyanate
foam
ammonium sulfate
parts
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
US07/210,748
Other languages
English (en)
Inventor
Kaneyoshi Ashida
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to US07/210,748 priority Critical patent/US4908161A/en
Assigned to FISCHER, HARRY, A. reassignment FISCHER, HARRY, A. ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: ASHIDA, KANEYOSHI
Priority to JP63261297A priority patent/JPH0220554A/ja
Priority to EP88202995A priority patent/EP0347497A3/en
Application granted granted Critical
Publication of US4908161A publication Critical patent/US4908161A/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/30—Sulfur-, selenium- or tellurium-containing compounds

Definitions

  • the present invention relates to fire retardants for isocyanate-based foams. More particularly, the present invention concerns fire retardants for flexible or rigid isocyanate-based foams. Even more particularly, the present invention concerns fire retardants for flexible and/or rigid polyurethane foams.
  • so-called flame retardant flexible polyurethane foams have been prepared by the addition of halogen- and/or phosphorous-containing flame retardants. While these foams pass small scale fire tests, they do not reflect actual fire conditions. Therefore, the tests can be used only as laboratory scale methods for screening.
  • foams classified as self-extinguishing foams as determined by the ASTM D-1692-59T test are flammable under actual fire conditions.
  • Another proposed method of making flame retardant flexible foams is high resilience foams (HR foams) which have lower melting points than conventional flexible urethane foams.
  • HR foams high resilience foams
  • These foams are prepared by using a blended polyisocyanate, e.g., 80%/20% mixture of TDI and polymeric MDI.
  • the low melting points of the foams result in a dripping phenomenon which prevents flame propagation.
  • the foams also can be classified as SE foams by the ASTM D-1692-59T, but these foams also are substantially flammable at actual fire conditions.
  • Substantially non-combustible flexible foams can be produced only by the addition of extremely large amounts of power-type flame retardants, and not by liquid type flame retardants.
  • the first commercial product of this type is a CMHR foam (combustion modified high resilience foam) developed by Mobay Chemical Corp. (J. F. Szabat and J. A. Gaetano, Proceedings of the SPI International Technical/Marketing Conference, Nov. 2-5, 1983, San Diego, pp. 326-331).
  • CMHR foam combustion modified high resilience foam
  • This type of foam employs alumina trihydrate as the major flame retardant.
  • methylolmelamine alkyl ethers have been taught as flame retardants for flexible urethane foams.
  • Melamine has been disclosed for rigid urethane foams in U.S. Pat. No. 4,221,875.
  • Cyanuric acid derivatives such as cyanamid, dicyandiamide, guanidine, biguanidine, and melamine have been disclosed as flame retardants for flexible urethane foams, as taught in U.S. Pat. No. 4,258,141.
  • the present invention is based on the finding that ammonium sulfate is an unexpectedly effective flame retardant for active-hydrogen containing isocyanate-based foams.
  • Ammonium sulfate is an inexpensive chemical ordinarily used as a fertilizer. However, Applicant is unaware of any teaching of ammonium sulfate as a flame retardant for urethane foams and the like.
  • flame retardant isocyanate-based foams and, in particular, flexible and rigid polyurethane foams are prepared by the incorporation thereinto of ammonium sulfate, as a fire retardant.
  • ammonium sulfate is, preferably, employed in powdered form. Because of the acidic nature of the sulfate, it is, ordinarily, admixed with a weakly basic powder to preclude adverse foam rise times.
  • Useful weakly basic powders include (a) alkali earth metal hydroxides, or (b) cyanuric acid derivatives, such as, cyanamide, melamine, and the like, as well as mixtures thereof. Generally, from about 5 to about 100 parts per weight of weakly basic powder per 100 parts per weight of ammonium sulfate is employed.
  • the fire retardant is incorporated into the foam formulation by any conventional technique, such as by mixing or the like. While being pre-eminently useful in the formation of flexible polyurethane foams, the fire retardant is, also, useful with rigid polyurethane foams, polyisocyanurate foams, carbodiimide foams and the like.
  • fire retardant active-hydrogen containing isocyanate-based foams are prepared by employing, as the fire retardant, ammonium sulfate. This result was completely unexpected in that ammonium sulfate, being acidic in nature, would be expected to impede foam formation.
  • ammonium sulfate is a widely known, commercially available solid inorganic chemical, usually employed as a fertilizer. It is water soluble and has a pH below 6.0. It has been found, however, that when used herein as a fine powder form, it is not water-soluble due to it being coated with urethane polymer or the like.
  • Useful weakly basic powder include (a) alkali earth metal hydroxides, (b) a cyanuric acid derivative thereof, as well as (c) mixtures thereof.
  • alkali earth metal hydroxide powders are magnesium hydroxide, calcium hydroxide, strontium hydroxide, barium hydroxide and mixtures thereof.
  • Useful derivatives of cyanuric acid include cyanamide, dicyandiamide, melamine, guanidine, biguanidine and the like and mixtures thereof.
  • the weakly basic powder is employed in an amount ranging from about 5 parts to about 100 parts by weight thereof per 100 parts of ammonium sulfate.
  • the weakly basic powder is employed in an amount ranging from about 10 to 30 parts by weight thereof per 100 parts by weight of ammonium sulfate. It should be noted, though, that these amounts can be varied, as required, by the foam formulation employed.
  • ammonium sulfate as a flame retardant is particularly advantageous in the formation of flame retardant flexible polyurethane foams.
  • flexible polyurethane foams are prepared by the reaction of an organic polyisocyanate with a polyhydric compound in the presence of catalyst, a surfactant and a suitable blowing agent, such as water, a halohydrocarbon or the like, as well as mixtures thereof.
  • Useful organic polyisocyanates for the preparation of urethane foams can be represented by the formula:
  • R is a polyvalent organic radical selected from the group consisting of aromatic, arylalkyl and alkylaryl organic radicals, as well as mixtures thereof; and Z is an integer corresponding to the valence number of R and is at least 2.
  • organic polyisocyanates contemplated herein include for example, the aromatic diisocyanates, such as 2,4-toluene diisocyanate, 2,6-toluene diisocyanate, mixtures of 2,4- and 2,6-toluene diisocyanate, crude toluene diisocyanate, methylene diphenyl diisocyanate, crude methylene diphenyl diisocyanate and the like; the aromatic triisocyanates such as 4,4',4"-triphenylmethane triisocyanate, the aromatic tetraisocyanates such as 4,4'-dimethyldiphenylmethane-2,2',5,5'-tetraisocyanate, and the like;
  • organic polyisocyanates include: hydrogenated methylene diphenylisocyanate, m-phenylene diisocyanate, naphthylene-1,5-diisocyanate, 1-methoxyphenyl-2,4-diisocyanate, 4,4'-biphenylene diisocyanate, 3,3'-dimethyl-4,4'-biphenyl diisocyanate, 3,3'-dimethyl-4,4'-biphenyl diisocyanate, and 3,3'-dimethyldiphenylmethane-4,4'diisocyanate, and the like.
  • polyisocyanates are prepared by conventional methods in the art such as the phosgenation of the corresponding organic amine.
  • Still another class of organic polyisocyanate useful herein are isocyanate-terminated quasi-prepolymers. These quasi-prepolymers are prepared by reacting excess organic polyisocyanate or mixtures thereof with a minor amount of an active hydrogen-containing compound. Suitable active hydrogen-containing compounds for preparing the quasi-prepolymers hereof are those containing at least two active hydrogen-containing groups which are isocyanate reactive.
  • Typifying such compounds are hydroxyl-containing polyesters, polyalkylene ether polyols, hydroxyl-terminated polyurethane polymers, polyhydric polythioethers, alkylene oxide adducts of phosphorus-containing acids, polyacetals, aliphatic polyols, aliphatic thiols including alkane, alkene and alkyne thiols having two or more --SH groups; as well as mixtures thereof.
  • Compounds which contain two or more different groups within the above-defined classes may also be used such as, for example, compounds which contain one --SH group and --OH group.
  • Still another class of useful polyisocyanates are carbodiimide-modified MDI; allophanate-modified TDI, urea-modified TDI, as well as oxazolidone-modified TDI.
  • Aliphatic polyisocyanates generally, are not suited for use herein because of their slow reaction rates.
  • the isocyanate have an isocyanate index of from about 90 to about 120.
  • polyhydric compounds are both polyester and polyether polyols.
  • Any suitable hydroxyl-containing polyester may be used such as are obtained, for example, from polycarboxylic acids and polyhydric alcohols.
  • Any suitable polycarboxylic acid may be used as oxalic acid, malonic acid, succinic acid, glutaric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, sebaic acid, brassylic acid, thapsic acid, maleic acid, fumaric acid, glutaconic acid, ⁇ -hydromuconic acid, ⁇ -hydromuconic acid, butyl- ⁇ -ethylglutaric acid, ⁇ , ⁇ -diethyl-succinic acid, phthalic acid, isophthalic acid, terephthalic acid, hemimetllitic acid, and 1,4-cyclohexanedicarboxylic acid.
  • Any suitable polydric alcohol including both aliphatic and aromatic may be used such as ethylene glycol, 1,3-propylene glycol, 1,2-propylene glycol, 1,4-butylene glycol, 1,3-butylene glycol, 1,2-butylene glycol, 1-5pentanediol, 1,4-pentanediol, 1,3-pentanediol, 1,6-hexanediol, 1,7-heptanediol, glycerol, 1,1,1-trimethylolpropane, 1,1,1-trimethylolethane, hexane-1,2,6-triol, ⁇ -methyl glucoside, pentaerythritol, and sorbitol.
  • polyhydric alcohol compounds derived from phenol such as 2,2-bis(4-hydroxyphenyl) propane, commonly known as Bisphenol A.
  • polyesters include lactone-based polyesters, such as those prepared by the ring polymerization of lactones, e.g. E-caprolactone.
  • Any suitable polyalkylene polyether polyol may be used such as the polymerization product of an alkylene oxide with a polyhydric alcohol. Any suitable polyhydric alcohol may be used such as those disclosed above for use in the preparation of hydroxyl-containing polyesters. Any suitable alkylene oxide may be used such as ethylene oxide, propylene oxide, butylene oxide, amylene oxide, and heteric or block copolymers of these oxides.
  • the polyalkylene polyether polyols may be prepared from other starting materials such as tetrahydrofuran and alkylene oxide tetrahydrofuran blends; epihalohydrins such as epichlorohydrin; as well as aralkylene oxides such as styrene oxide.
  • the polyalkylene polyether polyols may have either primary or secondary hydroxyl groups, and preferably, are polyethers prepared from alkylene oxides having from two to six carbon atoms such as polyethylene ether glycols, polypropylene ether glycols, and polybutylene ether glycols.
  • the polyalkylene polyether polyols may be prepared by any known process, such as, for example, the process disclosed in Wurtz in 1859 and Encyclopedia of Chemical Technology, vol. 7, pp. 257-262, published by Interscience Publishers, Inc. (1957) or in U.S. Pat. No. 1,922,459.
  • Any suitable polyhydric polythioether may be used such as, for example, the condensation product of thiodiglycol or the reaction product of a dihydric alcohol such as is disclosed above for the preparation of the hydroxy-containing polyesters with any other suitable thioether glycol.
  • the hydroxyl-containing polyester may also be a polyester amide such as is obtained by including some amine or amino alcohol in the reactants for the preparation of the polyesters.
  • polyester amides may be obtained by condensing an amino alcohol such as ethanolamine with the polycarboxylic acids set forth above, or they may be made using the same components that make up the hydroxyl-containing polyester with only a portion of the components that make up the hydroxyl-containing polyester with only a portion of the components being a diamine such as ethylene diamine.
  • Alkylene oxide adducts of acids of phosphorus which may be used include those neutral adducts prepared from the alkylene oxides disclosed above for use in the preparation of polyalkylene polyether polyol.
  • Acids of phosphorus which may be used are acids having a P 2 O 5 equivalency of from about 72 percent to about 95 percent. The phosphoric acids are preferred.
  • Any suitable polyacetal may be used such as, for example, the reaction product of formaldehyde or other suitable aldehyde with a dihydric alcohol or an alkylene oxide such as those disclosed above.
  • Any suitable aliphatic thiol including alkane thiols containing at least two --SH groups may be used such as 1,2-ethanedithiol, 1,2-propanedithiol, 1,3-propanedithiol, and 1,6-hexanedithiol, alkene thiols such as 2-butene-1,4-dithiol, and alkyne thiols such as 3-hexyne-1,6-dithiol.
  • hydroxy-terminated polyurethane polymers such as a hydroxy-terminated polymer made by reacting the isocyanate with several moles of an alkylene glycol.
  • Polymeric polyols such as those which are prepared by grafting styrene and/or acrylonitrile with polyether polyols can also be used, as well as polyurea dispersion polyols.
  • the preferable functionality of the polyols are in a range of between about 2 and 3, and their preferable hydroxyl equivalent weights are in a range of about 1,000 and 2,000, and have a hydroxyl number between about 25 and 56.
  • a chemical or physical blowing agent may be used.
  • Chemical blowing agents include, for example, water, crystal water-containing inorganic or organic salts, such as sodium sulfate decahydrate, sodium borate decahydrate and the like.
  • Organic blowing agents such as nitroethane, acetaldoxime, boric acid and the like may, also, be used. These blowing agents are described in the book "International Progress in Urethanes", V. 2, page 153, edited by K. Ashida and K. C. Frisch and published by Technomic Publishing Co., Inc. (1980).
  • the physical blowing agents are the halohydrocarbon blowing agents which include chlorofluorocarbons, such as trichloromonofluoromethane, hydrochlorofluorocarbons, such as dichlorotrifluoroethane, alkylene chlorides, such as methylene chloride, and the like.
  • chlorofluorocarbons such as trichloromonofluoromethane
  • hydrochlorofluorocarbons such as dichlorotrifluoroethane
  • alkylene chlorides such as methylene chloride, and the like.
  • pentane may be used as a blowing agent.
  • the blowing agent is present in an amount ranging from about 1 to about 50 parts, by weight thereof per 100 parts by weight of polyhydric compound.
  • the catalysts employed herein are the conventional catalysts used for making polyurethane foams.
  • the catalysts include both tin catalysts and tertiary amine catalysts.
  • Representative tin catalysts are dibutyltin dilauate and stannous octoate.
  • Commonly used tertiary amine catalysts include N-methylmorphorine, N,N,N',N'-tetramethylpropylene diamine, 1,4-diazabicyclo [2,2,2] octane, (DABCO), 1,8-diazabicyclo[5,4,0] undecene-7 and its salts such as the phenol salt, 2-ethylhexanoic acid salt and the like.
  • the catalyst is employed in catalytic amounts ranging from about 1 to 5 parts by weight thereof per 100 parts by weight of polyhydric compound.
  • the silicone surfactants used for the preparation of the flexible foams are well known and commercially available. Generally, they are polysiloxane-polyoxyalkylene block copolymers which are either linear or pendant block copolymers. Representative of this type of surfactant are those sold commercially by Dow Chemical under the name DC-193 and the like. Ordinarily, from about 0.1 to about 3.0 parts, by weight, of surfactant per 100 parts by weight of polyhydric compound are employed.
  • the preferred polyhydric compounds are polyether polyols and, in particular, the styrene and/or acrylonitrile grafted polyether polyols.
  • the preferred polyisocyanates are toluene diisocyanate, carbodiimide-modified diphenylmethane diisocyanate, and mixtures thereof.
  • the polyisocyanate and polyhydric compound are employed in an NCO/OH equivalent weight ratio ranging from about 0.9 to about 1.2.
  • the amount of ammonium sulfate required to impart flame retardancy can be calculated on the amount of polyhydric compound employed. Usually, at least 50 parts by weight of polyhydric compound per 100 parts by weight of polyhydric compound is employed. Preferably, from about 50 to about 150 parts by weight of ammonium sulfate powder per 100 parts by weight of polyhydric compound is employed.
  • the flexible foams are usually prepared at ambient conditions by adding the polyol, catalyst, surfactant, blowing agent and flame retardant, as one component, to the isocyanate and water, using conventional techniques.
  • the present flame retardant can be used for the manufacture of other active-hydrogen containing isocyanate-based foams, such as polyol-containing isocyanurate foams, isocyanurate-modified polyurethane foams, modified-carbodiimide foams, carbodiimide-isocyanurate foams and the like.
  • This example illustrates the preparation of a flexible polyurethane foam in accordance herewith. Using a suitable reaction vessel, with stirring, and at ambient conditions, various ingredients were added thereto and foam formation was observed.
  • Table I sets forth the ingredients and the observed physical properties.
  • This example illustrates the usage of a weakly basic powder with the ammonium sulfate.
  • the weakly basic powder, melamine was dispersed with the ammonium sulfate in the polyol and maintained at 70° C., with stirring, for about 15 hours prior to use.
  • Table II below sets forth the ingredients used and the resulting physical properties.
  • the so-prepared foams exhibited excellent flame retardance.
  • the California Test is one which simulates actual fire conditions and the excellence of the foams render these conditions is evident from the data. Also, by pre-heating the polyol, the rise time is increased, as well as by permitting the polyol with the sulfate dispersed therein to stand prior to use.
  • This example illustrates the preparation of a rigid polyurethane foam in accordance herewith.
  • the polyol, surfactant, fire retardant, and catalyst were admixed with the isocyanate and water.
  • Table VII below tabulates the formulation and the resulting physical properties.
  • flame retardant isocyanate-based foams can be achieved hereby, especially with respect to polyurethane foams.
  • the foams produced hereby are close-celled products which, if desired, can be either closed or open molded.
  • ammonium sulfate flame retardant with or without the weakly basic powder, can be used, alone, or in conjunction with other flame retardants.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
US07/210,748 1988-06-23 1988-06-23 Fire retardant for isocyanate-based foams comprising ammonium sulfate and a cyanuric acid derivative Expired - Fee Related US4908161A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
US07/210,748 US4908161A (en) 1988-06-23 1988-06-23 Fire retardant for isocyanate-based foams comprising ammonium sulfate and a cyanuric acid derivative
JP63261297A JPH0220554A (ja) 1988-06-23 1988-10-17 イソシアネート基材発泡体用の可燃抑制剤及びポリウレタン発泡体の製造方法
EP88202995A EP0347497A3 (en) 1988-06-23 1988-12-22 Fire retardant for isocyanate-based foams

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US07/210,748 US4908161A (en) 1988-06-23 1988-06-23 Fire retardant for isocyanate-based foams comprising ammonium sulfate and a cyanuric acid derivative

Publications (1)

Publication Number Publication Date
US4908161A true US4908161A (en) 1990-03-13

Family

ID=22784125

Family Applications (1)

Application Number Title Priority Date Filing Date
US07/210,748 Expired - Fee Related US4908161A (en) 1988-06-23 1988-06-23 Fire retardant for isocyanate-based foams comprising ammonium sulfate and a cyanuric acid derivative

Country Status (3)

Country Link
US (1) US4908161A (ja)
EP (1) EP0347497A3 (ja)
JP (1) JPH0220554A (ja)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5055208A (en) * 1991-01-02 1991-10-08 Powsus, Inc. Fire extinguishing compositions
US5135961A (en) * 1990-07-27 1992-08-04 Ethyl Corporation Stabilized flame retardant polyol composition
US5260344A (en) * 1992-03-13 1993-11-09 Asahi Glass Company, Ltd. Open cell rigid isocyanurate foams and method for producing the same and vacuum heat insulating layer by use of the same
US5296181A (en) * 1991-09-19 1994-03-22 Bayer Aktiengesellschaft Process for the production of composite bodies having enhanced bonding between layers of the composite bodies thus obtained
US5976000A (en) * 1996-05-28 1999-11-02 Micron Technology, Inc. Polishing pad with incompressible, highly soluble particles for chemical-mechanical planarization of semiconductor wafers
US20070197672A1 (en) * 2006-02-22 2007-08-23 Dow Global Technologies Inc. One-component flexible polyurethane foam compositions and methods for their use

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4026702A1 (de) * 1990-08-24 1992-02-27 Bayer Ag Verfahren zur herstellung von harten polyurethanschaumstoffen
JP6317916B2 (ja) * 2013-11-29 2018-04-25 中部電力株式会社 消火剤及び消火方法

Citations (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA539301A (en) * 1957-04-09 Aarons Ralph Flame retardant compositions
US2881088A (en) * 1956-03-22 1959-04-07 Alim Corp Fire retardant composition and method of coating therewith
DE2035072A1 (en) * 1970-07-15 1972-01-20 Correcta Werke Gmbh Polyurethane foam - contg ammonium sulphate as flame-retardant filler
US3737400A (en) * 1972-03-24 1973-06-05 Toyo Rubber Chemical Ind Co Self-extinguishable polyurethane foam
DE2161690A1 (de) * 1970-10-08 1973-07-12 Correcta Werke Gmbh Verminderung der gefahr von kernverbrennungen und rissbildungen bei der herstellung von bloecken und straengen aus polyurethan-hartschaum
JPS49134999A (ja) * 1973-05-01 1974-12-25
DE2542048A1 (de) * 1975-09-20 1977-03-24 Herbert Prignitz Herabsetzung der brennbarkeit von polyurethan-schaumstoff
US4272414A (en) * 1978-05-26 1981-06-09 Monsanto Company Chemical retardants for forest fires
US4301217A (en) * 1978-10-26 1981-11-17 Ciba-Geigy Corporation Method of flameproofing wood with inorganic ammonium salts and dicyandiamide/formaldehyde reaction products
US4419401A (en) * 1982-08-03 1983-12-06 Pearson Glenn A Fire retardant concentrates and methods
US4436841A (en) * 1982-05-26 1984-03-13 Bayer Aktiengesellschaft Single-phase, storage-stable polyol compositions containing salts and the use thereof in the production of polyurethanes
US4486468A (en) * 1982-08-27 1984-12-04 Anti-Fire-Foam, Inc. Fire retardant foam
US4552803A (en) * 1983-01-28 1985-11-12 Pearson Glenn A Fire retardant powders and methods
US4582524A (en) * 1979-07-12 1986-04-15 Skw Trostberg Aktiengesellschaft Non-caking granular mineral fertilizer and process for its production
US4723959A (en) * 1984-11-07 1988-02-09 Nitto Boseki Co., Ltd. Non-inflammable fiber materials and process for producing the same

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2815554A1 (de) * 1978-04-11 1979-10-25 Basf Ag Schwerentflammbare polyurethan-weichschaumstoffe

Patent Citations (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA539301A (en) * 1957-04-09 Aarons Ralph Flame retardant compositions
US2881088A (en) * 1956-03-22 1959-04-07 Alim Corp Fire retardant composition and method of coating therewith
DE2035072A1 (en) * 1970-07-15 1972-01-20 Correcta Werke Gmbh Polyurethane foam - contg ammonium sulphate as flame-retardant filler
DE2161690A1 (de) * 1970-10-08 1973-07-12 Correcta Werke Gmbh Verminderung der gefahr von kernverbrennungen und rissbildungen bei der herstellung von bloecken und straengen aus polyurethan-hartschaum
US3737400A (en) * 1972-03-24 1973-06-05 Toyo Rubber Chemical Ind Co Self-extinguishable polyurethane foam
JPS49134999A (ja) * 1973-05-01 1974-12-25
DE2542048A1 (de) * 1975-09-20 1977-03-24 Herbert Prignitz Herabsetzung der brennbarkeit von polyurethan-schaumstoff
US4272414A (en) * 1978-05-26 1981-06-09 Monsanto Company Chemical retardants for forest fires
US4301217A (en) * 1978-10-26 1981-11-17 Ciba-Geigy Corporation Method of flameproofing wood with inorganic ammonium salts and dicyandiamide/formaldehyde reaction products
US4582524A (en) * 1979-07-12 1986-04-15 Skw Trostberg Aktiengesellschaft Non-caking granular mineral fertilizer and process for its production
US4436841A (en) * 1982-05-26 1984-03-13 Bayer Aktiengesellschaft Single-phase, storage-stable polyol compositions containing salts and the use thereof in the production of polyurethanes
US4419401A (en) * 1982-08-03 1983-12-06 Pearson Glenn A Fire retardant concentrates and methods
US4486468A (en) * 1982-08-27 1984-12-04 Anti-Fire-Foam, Inc. Fire retardant foam
US4552803A (en) * 1983-01-28 1985-11-12 Pearson Glenn A Fire retardant powders and methods
US4723959A (en) * 1984-11-07 1988-02-09 Nitto Boseki Co., Ltd. Non-inflammable fiber materials and process for producing the same

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5135961A (en) * 1990-07-27 1992-08-04 Ethyl Corporation Stabilized flame retardant polyol composition
US5055208A (en) * 1991-01-02 1991-10-08 Powsus, Inc. Fire extinguishing compositions
WO1992011903A1 (en) * 1991-01-02 1992-07-23 Powsus, Inc. Fire-extinguishing compositions
US5296181A (en) * 1991-09-19 1994-03-22 Bayer Aktiengesellschaft Process for the production of composite bodies having enhanced bonding between layers of the composite bodies thus obtained
US5260344A (en) * 1992-03-13 1993-11-09 Asahi Glass Company, Ltd. Open cell rigid isocyanurate foams and method for producing the same and vacuum heat insulating layer by use of the same
US5976000A (en) * 1996-05-28 1999-11-02 Micron Technology, Inc. Polishing pad with incompressible, highly soluble particles for chemical-mechanical planarization of semiconductor wafers
US20070197672A1 (en) * 2006-02-22 2007-08-23 Dow Global Technologies Inc. One-component flexible polyurethane foam compositions and methods for their use
US7776934B2 (en) * 2006-02-22 2010-08-17 Dow Global Technologies Inc. One-component polyurethane foam compositions and methods for their use

Also Published As

Publication number Publication date
EP0347497A2 (en) 1989-12-27
JPH0220554A (ja) 1990-01-24
EP0347497A3 (en) 1990-03-21

Similar Documents

Publication Publication Date Title
EP0429103B1 (en) Soft flexible polyurethane foams, a process for preparing the same, and a polyol composition useful in said process
US4165414A (en) Urethane-modified isocyanurate foams having improved insulating and flame retardant properties
US4092276A (en) Process for the preparation of foams characterized by isocyanurate and urethane linkages
US3981829A (en) Process for the preparation of carbodiimide-isocyanurate foams
DE4446847A1 (de) Verfahren zur Herstellung von flammgeschützten Hartschaumstoffen auf Isocyanatbasis
JPS6248718A (ja) 難燃性軟質ポリウレタンフオ−ムの製造
US4849459A (en) Flame retardant polyurethane foams
US4129693A (en) Urethane-modified isocyanurate foams having enhanced physical properties
US4908161A (en) Fire retardant for isocyanate-based foams comprising ammonium sulfate and a cyanuric acid derivative
US4826884A (en) Flame retardant polyurethane foams resistant to cigarette smoldering ignition
US3994839A (en) Urethane modified carbodiimide foams derived from flame retardant polyols
US5830926A (en) Flame retardant polyurethane foams
US5730909A (en) Flame retardant polyurethane foams
DE2506657A1 (de) Verfahren zur herstellung von zellfoermigen schaumstoffen
US4892893A (en) Flame retardant polyurethane foams resistant to cigarette smoldering ignition
US3723366A (en) Carbodiimide foams and improved process for preparing same
US3969288A (en) Carbodiimide-isocyanurate foams prepared from acid-modified toluene diisocyanate
US3887501A (en) Process for the preparation of carbodiimide-isocyanurate foams
GB2133801A (en) Aminoplast resins dispersions and low flammability cellular and non-cellular polyurethane products prepared therefrom
US3891578A (en) Carbodiimide-isocyanurate foams containing urethane linkages
US3645923A (en) Carbodiimide foam composition and process for the preparation therefor
US3994837A (en) Urethane-modified carbodiimide-isocynurate foams prepared from TDI-rich isocyanates
US4051082A (en) Carbodiimide-isocyanurate foams modified with ethoxylated polyols
US4029611A (en) Carbodiimide-isocyanurate foams modified with polyfurfuryl alcohol polymers
DE19540809A1 (de) Verfahren zur Herstellung von flammwidrigen Polyurethan-Weichschaumstoffen

Legal Events

Date Code Title Description
AS Assignment

Owner name: FISCHER, HARRY, A., 65 AMBLESIDE DRIVE, BRAMPTON,

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:ASHIDA, KANEYOSHI;REEL/FRAME:004901/0742

Effective date: 19880616

Owner name: FISCHER, HARRY, A.,CANADA

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:ASHIDA, KANEYOSHI;REEL/FRAME:004901/0742

Effective date: 19880616

REMI Maintenance fee reminder mailed
LAPS Lapse for failure to pay maintenance fees
FP Lapsed due to failure to pay maintenance fee

Effective date: 19940313

STCH Information on status: patent discontinuation

Free format text: PATENT EXPIRED DUE TO NONPAYMENT OF MAINTENANCE FEES UNDER 37 CFR 1.362